A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17406984



Internal ID22464854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132229099..132231796hg38UCSC Ensembl
chr3:131947943..131950640hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg382698
hg192698
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5904815
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17406984
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer